Zemni Ines, Houissa Ines, Boujelbene Nadia, Sakhri Saida, Sassi Imene, Dhiab Tarek Ben
Department of Surgical Oncology, Salah Azaiez Institute, Faculty of Medicine of Tunis, University of Tunis El Manar, Boulevard 9 Avril 1938, Tunis, Tunisia.
University Tunis El Manar, Tunis, Tunisia.
J Med Case Rep. 2024 Oct 2;18(1):454. doi: 10.1186/s13256-024-04781-z.
Perivascular epithelioid cell tumors are uncommon mesenchymal tumors. The genital tract is the most common extrarenal location. Preoperative diagnosis is rarely achieved owing to non-specific symptoms and imaging features. Consensus on treatment strategies remains elusive. Case presentation We report the case a 38 year-old north African woman with a primary sterility, who was diagnosed with a uterine Perivascular epithelioid cell tumor of uncertain malignant potential on a resection specimen of an intracavity polypoid mass. Immunohistochemistry confirmed the diagnosis and we opted for conservative surgery to preserve the patient's fertility desires.
Uterine perivascular epithelioid cell tumor is a rare entity that warrants consideration in the differential diagnosis of uterine tumors. Treatment modalities, follow-up protocols, and prognosis remain ambiguous. Given their unpredictable behavior, accurate diagnosis and long-term monitoring are imperative.
血管周上皮样细胞瘤是一种罕见的间叶组织肿瘤。生殖道是肾外最常见的发病部位。由于症状和影像学特征不具特异性,术前很少能做出诊断。关于治疗策略的共识仍未达成。病例报告 我们报告一例38岁的北非女性,原发性不孕,在宫腔息肉样肿物的切除标本上被诊断为具有不确定恶性潜能的子宫血管周上皮样细胞瘤。免疫组化确诊了该诊断,我们选择了保守手术以满足患者保留生育能力的愿望。
子宫血管周上皮样细胞瘤是一种罕见疾病,在子宫肿瘤的鉴别诊断中值得考虑。治疗方式、随访方案和预后仍不明确。鉴于其行为不可预测,准确诊断和长期监测至关重要。